Medical Director overseeing endocrinology clinical trials and drug safety for Thermo Fisher Scientific. Providing medical monitoring, adverse - event review, regulatory support, and investigator consultation.
About the role
- Conseiller médical en oncologie chez Merck, pilotant le pipeline hématologique et les plans d’affaires médicales. Collaboration avec équipes cliniques, réglementaires, commerciales et scientifiques au Canada.
Responsibilities
- Manage scientific knowledge and provide strategic, medical, and scientific guidance for upcoming oncology indications, including solid and hematologic malignancies
- Develop, prioritize, and execute strategic and tactical Oncology Medical Affairs plans
- Identify medical and scientific gaps and prioritize tactics to address the needs of clinical scientific leaders
- Serve as the national point of contact for the regional Medical Affairs team
- Collaborate with global and regional teams to secure support for Canadian projects
- Support Phase II and III studies, local clinical evaluations, and investigator-initiated studies
- Encourage the conduct of clinical development studies in Canada
- Act as the medical point of contact for Market Access, Health Economics and Outcomes Research, Clinical Research, Marketing, and Regulatory Affairs
- Support the management of existing products and the launch of new products
- Participate in cross-functional brand teams and provide scientific expertise
- Support product approval submissions and the preparation of regulatory reports
- Establish professional relationships with key scientific leaders in Canada, regulatory agencies, payer groups, and patient advocacy organizations
- Share medical and scientific expertise with Regulatory Affairs, R&D, Quality Assurance, Legal, and Marketing teams
Requirements
- Pharm.D., M.D., or Ph.D.
- 2–3 years of experience as a Medical Science Liaison; experience as a Medical Advisor is preferred
- Knowledge of the pharmaceutical industry and the drug development process
- In-depth clinical knowledge of oncology
- Excellent understanding of strategic clinical development and study design principles for hematologic cancers
- Excellent oral and written communication skills
- Strong presentation and meeting facilitation skills
- High degree of ethics and integrity
- In-depth knowledge of Good Clinical Practice and Innovative Medicines Canada’s Code of Ethical Practices
- Ability to work effectively within a high-performing team and a matrix organizational structure
- Ability to interact with clinical researchers, contract research organizations, payer administrators, regulatory agencies, and patient advocacy organizations
- Fluency in French is required
- Required location: Quebec or Ontario
- Travel required: 25%
- Visa sponsorship is not available
- Regular employment status
Benefits
- Hybrid position
- Relocation: No relocation assistance
- Employment insurance/benefits: Not specified
- Time off and retirement plan: Not specified
- Equal opportunity employer
- Reasonable accommodations available throughout the recruitment process
- Opportunity to participate in Phase II and III studies, local clinical evaluations, and investigator-initiated studies
- Professional development opportunities through collaboration with regional and global teams
Job title
Job type
Experience level
Salary
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Degree requirement
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